Hey there, thanks for the add... Very much appreciate it. My name's Jamie (friends call me Jay) and I'm 27, I was diagnosed with RR MS on April 12th, 2003. Currently disabled, and am on Copaxone, but also have taken Rebif. (Rebif is EVIL!!!). Nah, it's all good, if you're on Rebif, and it works for you, that's awesome, I unfortunately was allergic to Rebif.

On a side note, not to scare anyone here... I was very shocked to have learned that MS is/was a terminal disease, but ceased being terminal when the treatments were founded. Royally PISSED no one told me this after 3 years until just recently, but, then again, as a friend said... would I really have wanted a doctor to tell me that at the time of my diagnosis? lmao, Nah...